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Naslov:Expression of DNA-damage response and repair genes after exposure to DNA-damaging agents in isogenic head and neck cells with altered radiosensitivity
Avtorji:ID Todorović, Vesna (Avtor)
ID Grošelj, Blaž (Avtor)
ID Čemažar, Maja (Avtor)
ID Prevc, Ajda (Avtor)
ID Nikšić Žakelj, Martina (Avtor)
ID Strojan, Primož (Avtor)
ID Serša, Gregor (Avtor)
Datoteke:.pdf PDF - Predstavitvena datoteka, prenos (2,75 MB)
MD5: 740BB6195938F15E29784163A65BEB60
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo OI - Onkološki inštitut Ljubljana
Povzetek:Background: Increased radioresistance due to previous irradiation or radiosensitivity due to human papilloma virus (HPV) infection can be observed in head and neck squamous cell carcinoma (HNSCC). The DNA-damage response of cells after exposure to DNA-damaging agents plays a crucial role in determining the fate of exposed cells. Tightly regulated and interconnected signaling networks are activated to detect, signal the presence of and repair the DNA damage. Novel therapies targeting the DNA-damage response are emerging; however, an improved understanding of the complex signaling networks involved in tumor radioresistance and radiosensitivity is needed. Materials and methods: In this study, we exposed isogenic human HNSCC cell lines with altered radiosensitivity to DNA-damaging agents: radiation, cisplatin and bleomycin. We investigated transcriptional alterations in the DNA-damage response by using a pathway-focused panel and reverse-transcription quantitative PCR. Results: In general, the isogenic cell lines with altered radiosensitivity significantly differed from one another in the expression of genes involved in the DNA-damage response. The radiosensitive (HPV-positive) cells showed overall decreases in the expression levels of the studied genes. In parental cells, upregulation of DNA-damage signaling and repair genes was observed following exposure to DNA-damaging agents, especially radiation. In contrast, radioresistant cells exhibited a distinct pattern of gene downregulation after exposure to cisplatin, whereas the levels in parental cells were unchanged. Exposure of radioresistant cells to bleomycin did not significantly affect the expression of DNA-damage signaling and repair genes. Conclusions: Our analysis identified several possible targets: NBN, XRCC3, ATR, GADD45A and XPA. These putative targets should be studied and potentially exploited for sensibilization to ionizing radiation and/or cisplatin in HNSCC. The use of predesigned panels of DNA-damage signaling and repair genes proved to offer a convenient and quick approach to identify possible therapeutic targets.
Ključne besede:DNA-damaging agents, gene expression, head and neck cancer, squamous cell carcinoma
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Datum objave:01.01.2022
Založnik:Association of Radiology and Oncology
Leto izida:2022
Št. strani:str. 173-184
Številčenje:Vol. 56, no. 2
Izvor:Ljubljana
PID:20.500.12556/DiRROS-19760 Novo okno
UDK:575:61
ISSN pri članku:1318-2099
DOI:10.2478/raon-2022-0014 Novo okno
COBISS.SI-ID:104343043 Novo okno
Avtorske pravice:by Authors
Datum objave v DiRROS:24.07.2024
Število ogledov:490
Število prenosov:168
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Radiology and oncology
Skrajšan naslov:Radiol. oncol.
Založnik:Slovenian Medical Society - Section of Radiology, Croatian Medical Association - Croatian Society of Radiology
ISSN:1318-2099
COBISS.SI-ID:32649472 Novo okno

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Jezik:Slovenski jezik
Ključne besede:poškodbe DNK, izražanje genov, rak glave in vratu, ploščatocelični rak


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